Prosthetic devices · 21 CFR 872 Subpart D
Polyacrylamide Polymer (Modified Cationic) Denture Adhesive
Call for PMAs 12/26/96 per 61 FR 50707 on 9/26/96
- Companies listing it
- 00 makers
- Brands and models
- 0
- 510(k) clearances
- 00 in five years
- FDA name
- Adhesive, Denture, Polyacrylamide Polymer (Modified Cationic)
Official records: FDA product classification for KON · 21 CFR 872.3480.
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026